The accessory role of the outer membrane porin protein MspD in Mycobacterium smegmatis zinc homeostasis.

IF 3.5 4区 生物学 Q3 MICROBIOLOGY
Elke Goethe, Martina Ackermann, Larissa Bulmann, Kristin Laarmann, Astrid Lewin, Janita Luehrs, Mathias Muesken, Ralph Goethe
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引用次数: 0

Abstract

Zinc is the second most abundant transition metal in living cells and is involved in numerous biological processes. Regulation of Mycobacterium smegmatis (MSMEG) zinc homeostasis and zinc-specific importers ZnuABC and ZnuABC2 in the mycobacterial cytoplasmic membrane are well described; however, transport across the outer membrane (OM) remained unexplored so far. MspD is a porin highly similar to MspA, the major and well-studied porin responsible for the uptake of several compounds. Unlike MspA and the paralogues MspB and MspC, MspD was found to be transcriptionally induced upon zinc starvation and deletion of the global Zinc Uptake Regulator ZUR. Our study aimed to investigate the role of mspD (msmeg_6057) in MSMEG zinc homeostasis as well as the regulation of MspD expression. In addition, by growth experiments, quantitative real-time PCR analyses, in situ gene tagging and electron microscopy, we successfully demonstrated the zinc-responsive expression of the MspD protein as well as its complex formation and incorporation into the OM. Overall, the results provided strong evidence for an involvement of the MspD protein in zinc homeostasis of MSMEG.

外膜孔蛋白MspD在耻垢分枝杆菌锌稳态中的辅助作用。
锌是活细胞中第二丰富的过渡金属,参与了许多生物过程。对耻垢分枝杆菌(MSMEG)锌稳态和锌特异性进口商ZnuABC和ZnuABC2在分枝杆菌细胞质膜中的调控进行了很好的描述;然而,到目前为止,通过外膜(OM)的运输仍未被探索。MspD是一种与MspA高度相似的孔蛋白,MspA是一种主要的、被充分研究的孔蛋白,负责几种化合物的吸收。与MspA及其类似物MspB和MspC不同,MspD被发现在锌饥饿和缺失全局锌摄取调节因子ZUR的情况下被转录诱导。本研究旨在探讨mspD (msmeg_6057)在mmsg锌稳态中的作用以及对mspD表达的调控。此外,通过生长实验、实时荧光定量PCR分析、原位基因标记和电镜观察,我们成功地证明了MspD蛋白的锌响应性表达及其复合物的形成和结合到OM中。总之,这些结果为MspD蛋白参与mmsg的锌稳态提供了强有力的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology-Sgm
Microbiology-Sgm 生物-微生物学
CiteScore
4.60
自引率
7.10%
发文量
132
审稿时长
3.0 months
期刊介绍: We publish high-quality original research on bacteria, fungi, protists, archaea, algae, parasites and other microscopic life forms. Topics include but are not limited to: Antimicrobials and antimicrobial resistance Bacteriology and parasitology Biochemistry and biophysics Biofilms and biological systems Biotechnology and bioremediation Cell biology and signalling Chemical biology Cross-disciplinary work Ecology and environmental microbiology Food microbiology Genetics Host–microbe interactions Microbial methods and techniques Microscopy and imaging Omics, including genomics, proteomics and metabolomics Physiology and metabolism Systems biology and synthetic biology The microbiome.
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